How to synthesize lactic anhydride

Abstract

Compounds of formula (Ia) and formula H n and an acid compound of formula X in a first solvent to produce a reaction mixture containing a compound of formula (Ib) and a lactic acid compound of formula (I) in a solution of the first solvent and / or water, wherein n is an integer other than 0, x is 0 or an integer other than 0, M is an alkali metal or alkaline earth metal, and X is a compound of formula H n The conjugate base of the acid compound of X. The resulting reaction mixture is filtered to produce a filtrate containing lactic acid in solution. The filtrate is crystallized from a second solvent to produce lactic anhydride.

Description

[Technical Field]

[0001] [CROSS-REFERENCE TO RELATED APPLICATIONS] This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application No. 63 / 019,870, filed May 4, 2020, the entire contents of which are incorporated herein by reference.

[0002] The present application and disclosed embodiments relate to improved methods, reactants, and reagents for the synthesis of lactic acid. More specifically, the present application and disclosed embodiments relate to improved methods, reactants, and reagents for the synthesis of lactic acid anhydride. [Background technology]

[0003] Lactic acid is a naturally occurring hydroxycarboxylic acid used in various industries for various purposes. For example, lactic acid is used as a food additive, detoxifier, and flavoring agent. Lactic acid is also a precursor for the chemical and polymer synthesis of biodegradable and biocompatible polymers. In cosmetics and personal care products, lactic acid is used for skin moisturization, acne prevention, and increasing skin collagen thickness (Non-Patent Document 1).

[0004] Global demand for lactic acid has been steadily increasing since 2013. In 2018, economic reports valued the global lactic acid market at US$ 2.64 billion, with an expected growth rate of 18.6% compound annual growth rate (CAGR) from 2019 to 2025 (see also Non-Patent Document 2 and Non-Patent Document 3).

[0005] Lactic acid is a chiral molecule consisting of two enantiomers: L-(+)-lactic acid or (S)-lactic acid and its mirror image, D-(-)-lactic acid or (R)-lactic acid. In the pharmaceutical industry, the purity and chemical structure of reactants and reagents can dramatically affect the resulting properties and therapeutic efficacy of active pharmaceutical ingredients (APIs). There are very few suppliers of high-quality lactic acid, especially lactic anhydride, suitable for API production. Most suppliers provide lactic acid as an approximately 80%–95% aqueous solution (e.g., approximately 90% aqueous solution). Aqueous lactic acid solutions contain significant impurities that make them unsuitable for API production.

[0006] The main method for preparing L-lactic acid involves the fermentation of carbohydrates followed by recovery and purification. Some of these methods are described in Patent Document 1 and other published literature (Non-Patent Document 4). For example, a lactic acid solution can be produced by converting crude lactic acid to calcium lactate by fermentation, crystallizing the calcium lactate, neutralizing the calcium lactate with a mineral acid (sulfuric acid), and filtering to obtain a lactic acid solution (Non-Patent Document 5). Another method for producing lactic acid involves fractional distillation of mixed ethers (ethyl ether and isopropyl ether) in over 50% of commercial syrups followed by crystallization (Non-Patent Document 4). These solvent extraction methods used to extract lactic acid from aqueous solutions suffer from low efficiency. Patent Document 2 describes the conversion of crude lactic acid to solid magnesium lactate, followed by acidification with hydrochloric acid gas to produce a lactic acid solution, from which lactic acid can be recovered using additional isolation and purification steps.

[0007] The preparation of anhydrous lactic acid often requires intensive and complex post-fermentation processes, typically including derivatization to Ca, Zn, or NH salts, isolation of the respective salts, acid treatment of the salts, distillation, crystallization, and additional isolation steps. One such method utilizes distillation under reduced pressure to obtain monomeric lactic acid, which is then subjected to adiabatic crystallization to obtain dry lactic acid crystals. See, for example, U.S. Patent No. 5,629,299; U.S. Patent No. 5,629,299; and U.S. Patent No. 5,629,299. [Prior art documents] [Patent documents]

[0008] [Patent Document 1] U.S. Patent No. 2,232,554

Patent document 2

Patent document 3

Patent document 4

Patent document 5

Non-licensed literature

[0009] [Non-licensed document 1] Philipp, Babilas; Ulrich, Knie; Christoph, Abels, "Cosmetic and dermatologic use of alpha hydroxy acids" Journal of German Society of Dermatology, 10(7):488-49, 2012 [Non-licensed document 2] Komesu, A., Oliveira, JAR d., Martins, LH d. S., Wolf Maciel, MR, and Maciel Filho, R., "Lactic acid production to purification: A review," BioResources. 12(2). 4364-4383, 2017 [Non-licensed document 3] Grand View Research, "Lactic Acid Market Size, Share & Trend Analysis Report" Report ID: 978-1-68038-126-9, 2019

Non-licensed Document 4

[0010] There are no known reliable processes available for isolating lactic anhydride directly into a non-aqueous solvent without going through an aqueous lactic acid solution. Also, there are no known processes for the chemical synthesis of lactic anhydride on an industrial scale that do not employ a complex number of inefficient steps that ultimately result in an aqueous or low-purity product. Therefore, improved methods for synthesizing lactic anhydride are needed to address the purity, complexity, and yield shortcomings of available conventional processes. [Means for solving the problem]

[0011] The present application and disclosed embodiments relate to improved methods, reactants, and reagents for synthesizing lactic acid on an industrial scale for all applications. More particularly, the present application and disclosed embodiments relate to improved methods, reactants, and reagents for synthesizing lactic acid anhydride for pharmaceutical applications.

[0012] In an exemplary embodiment, the compound of formula (Ia): [ka] and a compound of formula H n and an acid compound of Formula X in a first solvent to produce a reaction mixture comprising a compound of Formula (Ib) and a lactic acid compound of Formula (I) in a solution of the first solvent and / or water. [ka] wherein each n is independently an integer other than 0, x is 0 or an integer other than 0, M is an alkali metal or alkaline earth metal, and X is a group of formula H n It is the conjugate base of the acid compound of X.

[0013] In an exemplary embodiment, the lactic acid compound of Formula (I) is soluble in a first solvent and the compound of Formula (Ib) is insoluble in the first solvent. The resulting reaction mixture is filtered to produce a filtrate containing lactic acid in solution. The filtrate is crystallized from a second solvent to produce lactic anhydride.

[0014] The above and other objects, features and advantages of the present disclosure will become more readily apparent from the following detailed description of exemplary embodiments disclosed herein.

[0015] Embodiments of the present application will now be described, by way of example only, with reference to the accompanying drawings, in which: [Brief explanation of the drawings]

[0016] [Figure 1] FIG. 1 shows an exemplary reaction scheme for the synthesis of lactic anhydride. [Figure 2] FIG. 1 shows anhydrous lactic acid crystals produced using an exemplary synthesis scheme. [Figure 3] FIG. 1 shows an exemplary equipment layout for the synthesis of lactic anhydride. [Figure 4] FIG. 1 shows the H NMR results of the L-(+)-lactic acid final product synthesized using the exemplary synthetic scheme. [Figure 5] FIG. 1 shows representative chromatograms of standard solutions of D-lactic acid and L-lactic acid using the chiral HPLC protocol described herein. DETAILED DESCRIPTION OF THE INVENTION

[0017] The following examples and embodiments disclosed and described in this application are illustrative. Those skilled in the art will understand that various modifications to the embodiments may exist, including variations on the synthetic methods, processes, reactants, reagents, parameters, and conditions described herein, without departing from the scope or spirit of the application or the exemplary embodiments disclosed. This application relates to improved methods, reactants, and reagents for synthesizing lactic anhydride for use in industrial processes, including, but not limited to, petrochemical processes; chemical and polymer synthesis; processes for producing cosmetics and personal care products; processes for producing food additives, detoxifiers, and flavorings; and processes for producing pharmaceuticals and active pharmaceutical ingredients.

[0018] In an exemplary embodiment, the lactic anhydride compound of formula (I) is produced by the synthesis and process steps shown in Figure 1. The exemplary synthesis of Figure 1 can be used to produce lactic anhydride, particularly L-(+)-lactic acid, D-(-)-lactic acid, and DL-lactic acid.

[0019] 1, n is an integer other than 0, and x is 0 or an integer other than 0. In exemplary embodiments, n is 1 or 2, and x is 0-6.

[0020] M is an alkali metal or alkaline earth metal. Suitable alkali metals and alkaline earth metals include, but are not limited to, calcium, sodium, potassium, magnesium, lithium, cesium, barium, beryllium, or strontium. In an exemplary embodiment, M is calcium, and the compound of formula (Ia) is calcium lactate hydrate. In another exemplary embodiment, the compound of formula (Ia) is L-calcium lactate pentahydrate.

[0021] H nX is an acid. Suitable mineral acids include, but are not limited to, sulfuric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, perchloric acid, chloric acid, hydrofluoric acid, and nitric acid. Suitable organic acids include, but are not limited to, malonic acid, glutaric acid, citric acid, malic acid, tartaric acid, oxalic acid, or formic acid. In an exemplary embodiment, the acid is sulfuric acid or oxalic acid.

[0022] X is the conjugate base of the acid used in the synthesis of Figure 1. Depending on the acid used in the synthesis of Figure 1, the conjugate base may vary. A suitable example of a conjugate base is HSO4 -1 , Cl -1 , Br -1 , F -1 , I -1 , ClO4 -1 , ClO3 -1 , NO3 -1 , C2O2 -4 , C3H3O4 -1 , C5H6O4 -2 , C6H5O7 -3 , C4H5O5 -1 , C4H4O6 -2 , H2PO4 -1 or HCO2 - These include, but are not limited to:

[0023] In an exemplary step of the synthesis of FIG. 1, a compound of formula (Ia) is reacted with a compound of formula H n The compound is reacted with an acid compound of X in a first solvent. [ka]

[0024] The first solvent may be one or more ester-based solvents, including, but not limited to, methyl acetate, ethyl acetate, isopropyl acetate, or n-propyl acetate. Other suitable solvents include acetone, toluene, acetonitrile, methyl tert-butyl ether (MTBE), isopropanol, ethanol, methanol, tetrahydrofuran, butanol, butyl acetate, carbon tetrachloride, dichloroethane, dichloromethane, diethyl ether, diisopropyl ether, dimethyl sulfoxide, heptane, hexane, methyl acetate, ethyl ketone, methyl tert-butyl ether, or methyl isobutyl ketone. The first solvent can be selected based on the final use of the final lactic anhydride product. In an exemplary embodiment, the first solvent is methyl acetate, ethyl acetate, isopropyl acetate, and / or toluene.

[0025] a compound of formula (Ia) and a compound of formula H in a first solvent n The reaction of X with the acid compound produces a reaction mixture containing the compound of formula (Ib) and lactic acid (I) in solution in the first solvent and / or water. [ka]

[0026] Each n described herein is independently an integer other than 0. By way of example only, if the acid is HCl, H n If n in X is 1 and the acid is sulfuric acid, H n n in X is 2. By way of example only, when calcium lactate hydrate is used as formula (Ia) reacting with HCl, M n+ n is 2, and H n n in X is 1, [ka] In the formula (Ib), n is 2. By way of example only, when calcium chloride is used in the compound of formula (Ib), MX nwhere n is 2. In some embodiments, each n in the above formula has the same value based on stoichiometry. The stoichiometry and / or value of each n will be readily apparent to one of ordinary skill in the art.

[0027] In an exemplary embodiment, the compound of formula (Ib) is at least partially insoluble in the first solvent, and lactic acid (I) is at least partially soluble in the first solvent. In an exemplary embodiment, the compound of formula (Ib) is insoluble in the first solvent, and lactic acid (I) is soluble in the first solvent.

[0028] 1, the reaction mixture containing lactic acid (I) and the compound of Formula (Ib) in solution in the first solvent is filtered to concentrate a first filtrate containing lactic acid (I) in solution in the first solvent and / or water. The first filtrate containing lactic acid can be further processed, isolated, recovered, filtered, concentrated, distilled, decanted, crystallized, dried, and / or dehydrated to produce lactic anhydride.

[0029] Suitable filtration techniques include vacuum filtration, gravity filtration, cold filtration, hot filtration, Nutsche agitation filtration, centrifugal filtration, and robo-filtration. In an exemplary embodiment, gravity filtration is performed using a Buchner funnel. In another exemplary embodiment, gravity filtration is performed using a Kiriyama funnel. Buchner and Kiriyama funnels may be equipped with filter paper and filter cloth to facilitate filtration.

[0030] In an exemplary embodiment, after the first filtration, the first filtrate containing lactic acid in a solution of the first solvent and / or water can be distilled to remove the water and / or the first solvent and concentrate the lactic acid in the first filtrate. Removing as much of the first solvent and water from the first filtrate by distillation maximizes the yield of lactic anhydride.

[0031] After the initial filtration and distillation steps, the first filtrate containing lactic acid (I) is isolated, and then the lactic acid (I) is combined with a second crystallization solvent and crystallized by cooling the solution to produce purified crystals of anhydrous L-lactic acid (I). Optionally, seed crystals of lactic acid can be added to the solution to initiate and accelerate crystallization.

[0032] To maximize recovery and yield of the final product, the lactic acid is only partially soluble in the second crystallization solvent. The second crystallization solvent can be one or more solvents, including, but not limited to, toluene and heptane. An additional filtration step can be used to isolate and purify the resulting lactic anhydride product.

[0033] To increase the yield of lactic acid anhydride, other processing steps can be used after the first filtration step. For example, residual water can be removed from the isolated first filtrate by azeotropic removal of water to produce lactic acid anhydride. In an exemplary embodiment, azeotropic removal can be achieved by azeotropic distillation. A distillation solvent such as toluene can be used to form an azeotropic mixture with water to achieve azeotropic distillation. In an exemplary embodiment, a Dean-Stark water trap can be used to azeotropically remove water from the isolated first filtrate containing lactic acid in solution to produce dried lactic acid anhydride.

[0034] The degree of crystallization and purification of lactic anhydride obtained from a solution containing a crystallization solvent and lactic acid depends largely on the water content of the filtrate and the removal of water from the first filtrate produced after the initial filtration. In addition to the exemplary steps of synthesis disclosed herein, to increase the yield and purity of the lactic anhydride product, the water content of the filtrate can be monitored using Karl Fischer titration, and residual water can be removed azeotropically as described herein. In an exemplary embodiment, water can also be removed by drying the filtrate with a desiccant such as anhydrous Na2SO4. Water can also be removed from the first filtrate using molecular sieves and a drying oven.

[0035] Exemplary methods for synthesizing lactic anhydride disclosed herein can produce an anhydrous lactic acid product containing less than 0.1% by weight of water and less than 1% by weight of polylactic acid impurities, such as lactide, oligomers of lactic acid, and mixtures thereof. In some embodiments, the resulting anhydrous lactic acid is essentially free of water and polylactic acid and can be used in high-precision, high-purity industrial processes, such as the production of APIs. The resulting anhydrous lactic acid is substantially free of water and polylactic acid and can be used in high-precision, high-purity industrial processes, such as the production of APIs. As used herein, "substantially free of water and substantially free of polylactic acid" means that the product has less than about 5%, about 4%, about 3%, about 2%, about 1%, or about 0.5% water and / or polylactic acid.

[0036] In an exemplary embodiment of the synthesis of lactic anhydride shown in FIG. 1, calcium lactate hydrate can be neutralized with concentrated sulfuric acid in methyl acetate using Reaction Scheme 1. [ka]

[0037] Calcium lactate hydrate was used in Reaction Scheme 1, and methyl acetate (MeOAc) was selected as the solvent based on the end use of the lactic acid anhydride final product in the synthesis of active pharmaceutical ingredients (APIs). After reacting calcium lactate hydrate with concentrated sulfuric acid in methyl acetate, the resulting slurry containing lactic acid can be filtered and concentrated. Residual water can be removed by adsorption with calcium sulfate and azeotropic removal of the residual water using a rotary evaporator or vacuum distillation, including direct vacuum distillation, to produce the lactic acid anhydride final product.

[0038] In the exemplary embodiment of the synthesis of lactic acid anhydride of FIG. 1, calcium lactate hydrate can be neutralized with hydrochloric acid in methyl acetate using Reaction Scheme 2. [ka]

[0039] After reacting calcium lactate hydrate with hydrochloric acid, the resulting calcium chloride forms a hydrate that is insoluble in MeOAc, which can be filtered off. The filtrate containing lactic acid can be further processed by isolating the filtrate, collecting, filtering, concentrating, decanting, distilling, crystallizing, and / or dehydrating to produce high-purity lactic anhydride.

[0040] In the exemplary embodiment of the synthesis of lactic anhydride in FIG. 1, calcium lactate hydrate can be neutralized with oxalic acid in methyl acetate using Reaction Scheme 3 below. [ka]

[0041] Calcium lactate hydrate can be neutralized with oxalic acid, which has a pKa less than that of lactic acid. Reaction Scheme 3 utilizes a slurry-to-slice reaction in methyl acetate. Calcium oxalate is insoluble in methyl acetate and can be filtered off to yield a pure lactic acid filtrate. The pure lactic acid filtrate can be further processed by isolating the filtrate, collecting, filtering, concentrating, decanting, distilling, crystallizing, and / or dehydrating to produce high-purity lactic acid anhydride.

[0042] The final lactic anhydride product produced by Reaction Schemes 1 to 3 can be used to produce a compound of formula (XXII), i.e., 1-{6-[(4-fluorophenyl)methyl]-5-(hydroxymethyl)-3,3-dimethyl-1H,2H,3H-pyrrolo[3,2-b]pyridin-1-yl}-2-[(2R,5R)-5-methyl-2-{[(3R)-3-methylmorpholin-4-yl]]-2H,3H-pyrrolo[3,2-b]pyridin-1-yl ... The API compound of formula (XXIII) can be prepared by reacting 1-(6-(4-fluorobenzyl)-5-(hydroxymethyl)-3,3-dimethyl-2,3-dihydro-1H-pyrrolo[3,2-b]pyridin-1-yl)-2-((2R,5R)-5-methyl-2-(((R)-3-methylmorpholino)methyl)piperazin-1-yl)ethan-1-one (IUPAC name) or 1-(6-(4-fluorobenzyl)-5-(hydroxymethyl)-3,3-dimethyl-2,3-dihydro-1H-pyrrolo[3,2-b]pyridin-1-yl)-2-((2R,5R)-5-methyl-2-(((R)-3-methylmorpholino)methyl)piperazin-1-yl)ethan-1-one (name generated by ChemDraw Professional V.17.1.0.105(19)) with lactic anhydride in a solution of ethyl acetate. [ka]

[0043] Therefore, the formula (XXIII): [ka] 1. A method for preparing a compound of formula (I), comprising: Formula (XXII): [ka] with lactic anhydride as described herein to obtain a compound of formula (XXIII).

[0044] The following examples describe exemplary reaction conditions, parameters, and reagents for carrying out exemplary steps in the synthesis of lactic anhydride. The following examples illustrate some of the embodiments described herein. Those skilled in the art will understand that various modifications to the examples, including variations on the synthetic methods, processes, reactants, reagents, parameters, and conditions described herein, may exist without departing from the scope or spirit of the present application or the exemplary embodiments disclosed. The following examples can produce lactic anhydride products containing less than 0.1% by weight of water and less than 1% by weight of polylactic acid impurities, such as lactide, oligomers of lactic acid, and mixtures thereof. The examples can also be used to produce lactic anhydride, particularly L-(+)-lactic acid, D-(-)-lactic acid, and DL-lactic acid.

[0045] Abbreviation AcOH acetic acid EtOAc ethyl acetate h time IPAC or iPrOAc isopropyl acetate min Me methyl MeOAc Methyl acetate ROI ignition residue Tol Toluene [Example]

[0046] General steps: The following examples can be used to prepare high-purity lactic anhydride containing L-(+)-lactic acid, D-(-)-lactic acid, and / or DL-lactic acid. The following examples are for illustrative purposes only and are not intended to limit the scope of the embodiments and / or claims herein.

[0047] The chiral purity of the product was determined by an isocratic HPLC method using a chiral column with UV detection at 254 nm. This method was used in the release test of calcium L-lactate to determine the chiral purity and content of calcium D-lactate. The chemical structures of calcium L-lactate and calcium D-lactate are shown below. [ka]

[0048] Column: Phenomenex Chirex 3126 (D)-penicillamine, 4.6 mm ID x 250 mm L, 5 μm, product number 00G-3126-E0 Equipment: Agilent 1260 HPLC system with UV detector Mobile phase: 2 mmol / L CuSO4 in water:IPA (98:2) Column temperature: 30℃ Flow rate: 0.7mL / min Injection volume: 10μL Detector: 254 nm Needle Wash Solvent: Diluent Runtime: 40 minutes

[0049] The relative retention times (RRT) of D-lactic acid and L-lactic acid using this method were as follows:

[0050] TIFF0007731371000013.tif24170

[0051] Integration and calculation were performed by integrating only the peaks of L-lactic acid and D-lactic acid in the chromatogram. D-Calcium lactate (%) = [A D-乳酸 / (A L-乳酸 +A D-乳酸 )] x 100 Chiral purity (%) = 100 (%) - D-calcium lactate (%) * * Only if the D-lactic acid peak is 0.45% or higher is it taken into account in the calculation.

[0052] Figure 5 shows a representative chromatogram of the standard solution.

[0053] 1 1 H NMR data (including QNMR data) were obtained on a Varian Mercury 400 mHz machine.

[0054] Reaction Scheme 1: Use of concentrated H2SO4 as the mineral acid Example 1 In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (1.14 mL, 20.61 mmol, 0.9 equiv.) was added dropwise to a cold (-14°C) slurry of calcium lactate hydrate (5 g, 22.9 mmol, 1.0 equiv. on an anhydrous basis) and MeOAc (100 mL) in a flask under nitrogen. The slurry was stirred at -12°C for 30 minutes and then at room temperature for 2 hours. The resulting free-flowing slurry was then filtered, and the filtrate was concentrated to produce 3.79 g (quantitative) of a viscous liquid. The filtrate from Example 1 can be further processed by isolating the filtrate, collecting, filtering, concentrating, decanting, distilling, crystallizing, and / or dehydrating the filtrate to produce lactic anhydride.

[0055] Example 2: In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (1.27 mmol, 22.9 mmol, 1.0 equiv.) was added dropwise to a cold (-14 °C) slurry of calcium lactate hydrate (10 g, 34.45 mmol, 1.5 equiv. based on 4H2O) and MeOAc (100 mL) in a flask under nitrogen. The reaction mixture was stirred at -12 to -14 °C for 3 hours and then at room temperature for an additional 2 hours. The resulting slurry was then filtered through a sintered funnel and concentrated to approximately 3 volumes on a rotary evaporator. Five volumes of heptane were then slowly added, resulting in the formation of an oily, immiscible bottom layer in the reaction mixture. The reaction mixture was then concentrated to 3 volumes. Five volumes of heptane were then added, resulting in a similar oily bottom layer. The reaction mixture was then completely concentrated to a viscous oil, dissolved in 50 mL of MeOAc, and dried over anhydrous Na2SO4. The mixture was then concentrated to 2 volumes. Two volumes of heptane were added, followed by lactic acid seed crystals. Commercially available lactic anhydride was used as the seed in the first experiment, and the material from Example 2 or commercially available lactic anhydride was used as the seed in subsequent experiments. The reaction mixture was then cooled in an ice bath with stirring to obtain a semi-solid sludge containing some white crystals. The semi-solid sludge was then completely concentrated and subjected to high vacuum filtration to produce 3.57 grams of lactic anhydride as a hygroscopic white solid. This synthesis yielded 86.5% by weight of lactic anhydride.

[0056] Example 3: In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (3.06 mL, 55.12 mmol, 1.0 equiv.) was added dropwise to a cold (-13 °C) slurry of calcium lactate hydrate (20 g, 68.9 mmol, 1.25 equiv. based on 4H2O) and MeOAc (200 mL) in a flask under nitrogen. The slurry was stirred at -10 °C to -14 °C for 3 hours and then at room temperature for an additional 2 hours. The free-flowing slurry was then filtered through a short pad of anhydrous Na2SO4 in a sintered funnel and concentrated to approximately 2 volumes on a rotary evaporator. The solution was then cooled to 0 °C, after which 1.5 volumes of heptane were slowly added with stirring. At this point, L-lactic acid seed crystals and an additional 4.5 volumes of heptane (6 volumes total) were added. The resulting bilayer was then completely concentrated to a semi-solid sludge. This semi-solid was dissolved in 2 volumes of MeOAc and 10 volumes of heptane was slowly added. An immiscible layer formed at the bottom of the mixture. The mixture was then concentrated to 2 volumes, and 10 volumes of heptane was added, followed by additional lactic acid seed crystals. A lumpy slurry formed, which was completely concentrated to yield white, hygroscopic solid crystals of anhydrous L-lactic acid. This synthesis yielded 9.47 grams of 95.4 wt% anhydrous L-lactic acid.

[0057] Example 4: In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (275.6 mmol, 1.0 equiv.) was added dropwise over 15 minutes to a cold (-13°C) slurry of calcium lactate hydrate (100 g, 344.56 mmol, 1.25 equiv. based on 4H2O) and MeOAc (800 mL) in a flask under nitrogen. The slurry was stirred at a temperature of -12°C to -14°C for 6 hours. The slurry was then filtered through a Buchner funnel equipped with filter paper and filter cloth. The filter cake was washed with MeOAc (50 mL x 2) to obtain a total volume of 1000 mL of filtrate. The filtrate was then separated into the following fractions by measuring with a graduated cylinder: 1. Fraction A: 300 mL of the filtrate was used for crystallization from heptane / MeOAc. 2. Fraction B: 300 mL of the filtrate was used for crystallization from toluene / MeOAc. 3. Fraction C: 300 mL of the filtrate was used for crystallization from aqueous solution. 4. Fraction D: 95 mL was left unused.

[0058] Fraction A: The aqueous filtrate from Fraction A was concentrated to 30 mL, cooled to 0-5°C in an ice bath, and 60 mL of heptane was added dropwise to form an oily, immiscible layer. At this point, 30 mg of lactic anhydride crystals were added and immediately dissolved. The entire solution was then concentrated to 30 mL. 60 mL of heptane was added and concentrated to 30 mL, and this was repeated three times. 60 mL of heptane was then added, cooled in an ice bath, and 30 mg of lactic anhydride was added as seed crystals to form a slurry. The slurry was not free-flowing or filterable. The slurry was again completely concentrated on a rotary evaporator, dissolved in 10 mL of MeOAc, cooled in an ice bath, and then seed crystals and 60 mL of heptane were added to produce a slurry with good filtration properties. The slurry was then completely concentrated to yield a white solid of L-lactic anhydride adhering to the wall. This synthesis yielded 12.2 grams of 82% by weight L-lactic anhydride.

[0059] Fraction B: The aqueous filtrate from Fraction B was concentrated to 30 mL and cooled to 0-5°C in an ice bath. 60 mL of toluene was then added dropwise over 15 minutes. An immiscible oil layer formed after the addition of 60 mL of toluene. The two layers were then concentrated to 30 mL. 60 mL of toluene was added to this solution, and the mixture was concentrated to 30 mL at 30°C. This process was repeated three times. Finally, 60 mL of toluene was added, and the solution was cooled to 0-5°C in an ice bath. 30 mg of lactic anhydride seed crystals were added. The solution rapidly formed floating crystals, including large chunks of lactic anhydride. The solution was stirred until the large chunks of lactic anhydride broke up, forming a free-flowing, filterable slurry. The slurry was then filtered under nitrogen, yielding white crystals of lactic anhydride. This synthesis yielded 11.6 grams of 78% by weight lactic anhydride.

[0060] Fraction C: The aqueous filtrate from fraction C was completely concentrated to a viscous liquid and divided into two 6 g portions in 15 mL centrifuge tubes. Then, 600 μL of HO was added to both portions to make approximately 90% aqueous solutions. The solution was then cooled to 15 °C, and lactic anhydride seed crystals were added. The seeds dissolved at this temperature. The solution was then gradually cooled to 10 °C, and additional lactic anhydride seed crystals were added to obtain a slurry. The slurry was then placed in a refrigerator at 6 °C, where the seeds grew into larger crystals. The slurry was then centrifuged at 5 °C and 3000 rpm for 15 minutes. The resulting solid, including the crystals, was then collected by decantation and dried in a vacuum oven at room temperature. A total of 3.9 g (29% yield) of solid was recovered. These crystals were more difficult to transfer and dry than fractions B and C. The supernatant liquid present in the wet crystals was azeotroped with toluene (20 mL x 4). The resulting biphasic suspension was cooled to 0 °C with 20 mL of toluene, and lactic acid seed crystals were then added. A slurry was formed which was diluted twice with 20 mL of toluene. The resulting free-flowing slurry was filtered under nitrogen to yield 9.1 grams of 61 wt % lactic anhydride in the form of white crystals.

[0061] Example 5: In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (15 mL, 275.6 mmol, 1.0 equiv.) was added dropwise over 30 minutes to a cold (-15°C) slurry of calcium lactate hydrate (100 g, 344.56 mmol, 1.25 equiv. based on 4H2O) and MeOAc (800 mL) in a flask under nitrogen. The slurry was stirred at -12 to -14°C for 6 hours. The slurry was then filtered through a Buchner funnel equipped with filter paper and filter cloth. The filter cake was washed with 100 mL of MeOAc. The filtrate was concentrated to 300 mL. 200 mL of toluene was added, and the slurry was concentrated to 300 mL at 30°C. This process was repeated three times. The resulting bilayer was cooled to 4°C in an ice bath and centrifuged at 400 rpm while adding lactic anhydride crystals (50 mg) as seed. A clumpy solid immediately formed. The suspension was stirred at room temperature for 15 hours. A sticky slurry formed that was not free-flowing or filterable. Two volumes of MeOAc were added to dissolve all solids, and the solution was concentrated to a viscous oil on a rotary evaporator. One volume of MeOAc and two volumes of toluene were added to the solution, and it was concentrated to two volumes. Two more volumes of toluene were added, and it was concentrated to three volumes. At this point, a free-flowing slurry formed, which was filtered under vacuum and dried under high vacuum for four hours to yield 37.2 grams of 75 wt. % lactic anhydride in the form of a white crystalline solid. The water content of the lactic anhydride product, as determined by Karl Fischer titration, was 0.562 wt. %. Figure 2 shows the resulting lactic anhydride product of the synthesis.

[0062] Example 6: In an exemplary embodiment of Reaction Scheme 1, concentrated H2SO4 (15.0 mL, 275.6 mmol, 1.0 equiv.) was added dropwise over 30 minutes to a cold (-13°C) slurry of calcium lactate hydrate (100 g, 344.56 mmol, 1.25 equiv. based on 4H2O) and MeOAc (800 mL) in a flask under nitrogen. The slurry was stirred at a temperature of -10°C to -12°C for 6 hours. The slurry was then filtered through a Buchner funnel equipped with filter paper and filter cloth. The filter cake was washed with 100 mL of MeOAc. The filtrate was concentrated to 100 mL. 200 mL of MeOAc was added, concentrated to 100 mL, and repeated. 200 mL of toluene was added, concentrated to 300 mL at 30°C, and repeated three times. 200 mL of toluene was added. The resulting two layers were stirred at room temperature, and lactic anhydride crystals (50 mg) were added as seed crystals. A sludge-like slurry was formed that was not free-flowing or filterable. The slurry was concentrated to 100 mL at a temperature of 30° C. 200 mL of toluene was added and concentrated to 100 mL, which was repeated twice. At this point, a free-flowing slurry was formed, which was filtered under vacuum and dried under high vacuum at room temperature for 24 hours to yield 40.8 grams of 82 wt % lactic anhydride in the form of a white crystalline solid.

[0063] Using Reaction Scheme 1 and sulfuric acid, high-quality, high-purity, and high-yield lactic anhydride was produced from a slurry of calcium lactate hydrate. The slurry produced by Reaction Scheme 1 was easily filtered, and lactic acid was isolated in high yield as a purified final product. Exemplary Reaction Scheme 1 can produce high-purity and high-yield lactic anhydride.

[0064] Reaction Scheme 3: Use of solid oxalic acid as the neutralizing acid Example 7 In an exemplary embodiment of Reaction Scheme 3, solid anhydrous oxalic acid (1.39 g, 15.5 mmol, 0.9 equivalents) was added to a cold (−10° C.) slurry of calcium L-lactate hydrate (5 g, 1.0 equivalent, x mmol based on 4HO) in MeOAc (100 mL). The resulting slurry was stirred at −10° C. for 40 minutes, followed by stirring at room temperature for 46 hours. The slurry was then filtered through a sintered funnel and concentrated on a rotary evaporator to produce 2.63 g of 94 wt. % lactic acid in the form of a thick, viscous liquid. The filtrate containing lactic acid can be further processed by isolating, collecting, filtering, concentrating, decanting, distilling, crystallizing, and / or dehydrating the filtrate to produce high-purity anhydrous lactic acid.

[0065] Example 8 In an exemplary embodiment of Reaction Scheme 3, solid anhydrous oxalic acid (2.48 g, 27.54 mmol, 0.8 equiv.) was added to a cold (−10° C.) slurry of calcium L-lactate hydrate (10 g, 1.0 equiv., 17.22 mmol based on 4HO) in MeOAc (200 mL). The resulting slurry was warmed to room temperature and stirred at room temperature for 18 hours. The slurry was then filtered through a sintered funnel and concentrated to 5 volumes on a rotary evaporator to produce a filtrate. Five volumes of heptane, followed by lactic acid seed crystals, were added to the filtrate. A sludge formed, which was completely concentrated and placed under high vacuum to produce 3.86 g of 79 wt. % anhydrous L-lactic acid in the form of a white crystalline solid.

[0066] In exemplary Reaction Scheme 3, high-purity lactic anhydride, including L-(+)-lactic acid, D-(-)-lactic acid, and / or DL-lactic acid, can be produced in high yield.

[0067] Exemplary large-scale synthesis route (II) can be used to produce L-lactic anhydride containing less than 0.1 wt. % water and less than 1 wt. % polylactic acid impurities, such as lactide, oligomers of lactic acid, and mixtures thereof. [ka]

[0068] FIG. 3 shows an exemplary equipment layout for the synthesis of lactic anhydride using synthetic route II.

[0069] The apparatus used in Figure 3 includes two 80 L glass reactors (Reactor 1 and Reactor 2) and a tray dryer. The reactors are equipped with stirring devices. A filter flask is used for filtration. Vacuum filtration or pressure filtration can also be used.

[0070] Typical reactants, solvents and materials for carrying out synthetic route II are outlined in Table 1.

[0071] [Table 1]

[0072] In synthetic route II, the oxygen content in reactor 1 is reduced to 1% (by volume) or less before the reactants are charged to reactor 1. In an exemplary embodiment, the oxygen content in the reactor before the start of the reaction is 0.7%.

[0073] Reactor 1 is charged with 34.7 kg of isopropyl acetate and the agitator is started. The reactor is then charged with 7.5 kg of anhydrous calcium L-lactate. The reaction mixture is maintained at a temperature between 0°C and 10°C. In an exemplary embodiment, the reaction mixture is cooled and maintained at 7.3°C.

[0074] Then, 2.8 kg of sulfuric acid is charged into the reactor at a temperature of 0°C to 10°C. The reaction temperature is maintained at 0°C to 10°C throughout the reaction. After 3 hours, QNMR 1 The assay was continued until the result was 11.5 or greater, or the difference between two consecutive samples was 0.5% or less. 1 Analyze samples of the mixture using H-NMR spectroscopy every 1 to 4 hours.

[0075] In an exemplary embodiment, the reaction is carried out for 7 hours and 10 minutes, and QNMR 1 Assay by QNMR yielded 8.8%. 2The assay yielded 8.5%, with a difference of 0.3% between two consecutive samples. The peak area of ​​the lactic acid peak at 4.07 ppm was monitored for quantitative NMR analysis. QNMR was used for quantitative 1 HNMR is shown and the amount of test material was quantified (assayed) against an internal reference standard, which in this case was 1,3,5-trimethoxybenzene.

[0076] The reaction mixture is then filtered using a filter flask in a first filtration to produce a filter cake. Vacuum filtration can be used.

[0077] A second charge of 13.9 kg of isopropyl acetate is made to reactor 1 at a temperature of 0° C. to 30° C. In an exemplary embodiment, a second charge of isopropyl acetate is made to reactor 1 at a temperature of 3.7° C. to 6.4° C. The isopropyl acetate is cooled to a temperature of 0° C. to 10° C. In an exemplary embodiment, the mixture is cooled to a temperature of 6.3° C.

[0078] The filter cake from the first filtration was added to Reactor 1 at a temperature of 1° C. to 10° C. In an exemplary embodiment, the filter cake was added to Reactor 1 at a temperature of 6.3° C. to 6.4° C. The reaction mixture is stirred for 1 hour to 2 hours at a temperature of 0° C. to 10° C. In an exemplary embodiment, the reaction mixture is stirred for 1 hour and 3 minutes at a temperature of 6.4° C. to 8.7° C.

[0079] In the second filtration, the reaction mixture is filtered using a filter flask. The filtrate from the first filtration and the filtrate from the second filtration are added in small portions to reactor 2 through a capsule filter.

[0080] The mixture in reactor 2 is concentrated under reduced pressure (P≦−0.08 MPa) at or below 45° C. until 0.5 to 1.0 volumes remain. In an exemplary embodiment, the mixture is concentrated at a temperature between 16.5° C. and 32° C. and a pressure of −0.08 MPa.

[0081] Reactor 2 was further charged with 6.9 kg of isopropyl acetate and stirred until completely dissolved. The mixture was sampled and the water content determined using Karl Fischer titration. The mixture was cooled to a temperature of 20°C to 25°C. In an exemplary embodiment, the mixture was cooled to a temperature of 24.3°C.

[0082] Anhydrous L-lactic acid seed crystals are added to the mixture. In an exemplary embodiment, 30.0 g of anhydrous L-lactic acid seed crystals are added to the mixture over 1 to 2 hours at a temperature of 20°C to 25°C. The mixture is stirred for 1 to 2 hours at a temperature of 20°C to 25°C. In an exemplary embodiment, the mixture is stirred for 1 to 2 hours at a temperature of 21.4°C to 24.2°C.

[0083] The mixture is cooled to a temperature of 0°C to 10°C. In an exemplary embodiment, the mixture is cooled to a temperature of 9.5°C. The mixture is stirred at a temperature of 0°C to 10°C for 1 to 2 hours. In an exemplary embodiment, the mixture is stirred at a temperature of 2.3°C to 9.5°C.

[0084] Toluene is added to the mixture through a capsule filter at a temperature between 0° C. and 10° C. In an exemplary embodiment, 52.2 kg of toluene is added to the mixture through a capsule filter at a temperature between 0° C. and 10° C.

[0085] The mixture is stirred for 2 to 3 hours at a temperature between 0° C. and 10° C. In an exemplary embodiment, the mixture is stirred for 2 to 3 hours at a temperature between 1° C. and 2.8° C.

[0086] The mixture was filtered using a filter flask. The filter cake was rinsed twice with 6.3 kg of toluene. The solids from the filter were placed in a tray dryer and dried at 15-25°C for 12 hours. In an exemplary embodiment, the drying temperature is 20-21°C. The solids were sampled for residual solvent analysis every 4-12 hours until the residual isopropyl acetate was 5000 ppm or less and the residual toluene was 890 ppm or less. In an exemplary embodiment, the product contained 563 ppm isopropyl acetate and 277 ppm toluene.

[0087] The resulting product is L-lactic acid anhydride. In an exemplary embodiment, the resulting product is 6.0 kg of 99.3 wt % L-lactic acid anhydride ( 1 (Based on H-NMR spectroscopy). The yield of synthetic route II is at least 47% with 100% chiral purity.

[0088] The reaction scale and yield of two batches of L-lactic anhydride produced by synthetic route II are presented in Table 2.

[0089] [Table 2]

[0090] Tables 3 and 4 summarize the chemical properties of the lactic anhydride final products of batches 1 and 2.

[0091] [Table 3]

[0092] [Table 4]

[0093] Figure 4 shows the final product L-(+)-lactic acid synthesized using synthetic route II. 1 The HNMR results are shown below.

[0094] The exemplary synthesis and reaction schemes disclosed herein can be used to produce lactic anhydride, particularly L-(+)-lactic acid, D-(-)-lactic acid, and DL-lactic acid, for use in industrial processes including, but not limited to, petrochemical processes; chemical and polymer synthesis; processes for producing cosmetics and personal care products; processes for producing food additives, detoxifiers, and flavorings; and processes for producing pharmaceuticals and active pharmaceutical ingredients.

Claims

1. 1. A method for synthesizing lactic anhydride comprising the steps of: [Chemical 1] and a compound of formula H ｎ and an acid compound of X in a first solvent to form a reaction mixture comprising a compound of Formula (Ib) and a lactic acid compound of Formula (I) in solution in the first solvent; 【Chemistry 2】 wherein each n is independently an integer other than 0, x is 0 or an integer other than 0, M is an alkali metal or alkaline earth metal, and X is a group represented by the formula H ｎ and the first solvent is one or more solvents selected from an ester solvent, acetone, toluene, acetonitrile, methyl tert-butyl ether (MTBE), isopropanol, ethanol, methanol, tetrahydrofuran, butanol, butyl acetate, carbon tetrachloride, dichloroethane, dichloromethane, diethyl ether, diisopropyl ether, dimethyl sulfoxide, heptane, hexane, ethyl ketone, or methyl isobutyl ketone. filtering the reaction mixture to produce a filtrate containing the lactic acid compound of formula (I) in solution; crystallizing the filtrate from a second solvent to produce a crystallized product; A method comprising:

2. The method of claim 1 further comprising concentrating the filtrate.

3. 3. The method of claim 2, wherein concentrating the filtrate comprises distilling the filtrate.

4. 2. The method of claim 1, wherein the lactic acid compound of formula (I) is soluble in the first solvent.

5. 10. The method of claim 1, wherein the compound of formula (Ib) is insoluble in the first solvent.

6. 10. The method of claim 1, wherein M is calcium.

7. 2. The method of claim 1, wherein M is selected from the group consisting of sodium, potassium, magnesium, lithium, barium, beryllium, cesium, and strontium.

8. Formula H ｎ 2. The method of claim 1, wherein the acid compound of X is sulfuric acid and X is a sulfate.

9. Formula H ｎ 2. The method of claim 1, wherein the acid compound of X is oxalic acid and X is oxalate.

10. Formula H ｎ 2. The method of claim 1, wherein the acid compound of X is hydrochloric acid and X is chloride.

11. 2. The method of claim 1, wherein the compound of formula (Ia) is calcium L-lactate hydrate.

12. The method of claim 1 , wherein the first solvent is an ester-based solvent.

13. 13. The method of claim 12, wherein the ester solvent is methyl acetate.

14. 13. The method of claim 12, wherein the ester solvent is ethyl acetate.

15. 13. The method of claim 12, wherein the ester solvent is isopropyl acetate.

16. The method of claim 12, wherein the ester solvent is n-propyl acetate.

17. 2. The method of claim 1, wherein the first solvent is selected from the group consisting of acetone, toluene, acetonitrile, MTBE, isopropanol, ethanol, methanol, and tetrahydrofuran.

18. The method of claim 1 , wherein the second solvent is toluene.

19. 10. The method of claim 1, wherein the second solvent is heptane.

20. 10. The method of claim 1, further comprising introducing seed crystals of lactic anhydride into the second solvent during crystallization.

21. 10. The method of claim 1, further comprising azeotropically removing water from the filtrate.

22. 10. The method of claim 1, further comprising vacuum drying the crystallized product.

23. The method of claim 1 further comprising drying the filtrate with a desiccant.

24. The desiccant is Na ２ SO ４ 24. The method of claim 23, wherein:

25. 2. The method of claim 1, wherein the lactic anhydride is L-(+)-lactic anhydride.

26. 2. The method of claim 1, wherein the lactic anhydride is D-(-)-lactic acid or DL-lactic acid.

27. A method for synthesizing lactic acid anhydride, comprising reacting calcium lactate anhydride with an acid in an ester solvent.

28. 28. The method of claim 27, wherein the acid is sulfuric acid.

29. 28. The method of claim 27, wherein the ester solvent is isopropyl acetate.

30. 28. The method of claim 27, wherein the lactic anhydride is L-(+)-lactic anhydride.

31. 28. The method of claim 27, wherein the lactic anhydride is D-(-)-lactic acid or DL-lactic acid.

32. 10. The method of claim 1, wherein the lactic anhydride contains less than 1% by weight of polylactic acid impurities.

33. 28. The method of claim 27, wherein the lactic anhydride contains less than 0.1% by weight of water.

34. 28. The method of claim 27, wherein the lactic anhydride contains less than 1% by weight of polylactic acid impurities.

35. Formula (XXIII): 【Chemistry 3】 2. A method for preparing a compound of formula (XXII): 【Chemistry 4】 with the lactic anhydride of claim 1 to obtain the compound of formula (XXIII).

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